神经纤维瘤病
医学
神经纤维瘤
丛状神经纤维瘤
神经鞘瘤
腰骶关节
周围神经鞘恶性肿瘤
神经纤维蛋白1
神经鞘肿瘤
外科
病理
神经鞘瘤
作者
Akshay Pratap,Pravin Nepal,Amit Agrawal,Mahi Pal Singh,Sagar Pandey
出处
期刊:Pediatric Neurosurgery
[S. Karger AG]
日期:2007-01-01
卷期号:43 (5): 410-413
被引量:6
摘要
Malignant peripheral nerve sheath tumors (MPNSTs) are the leading cause of death in young adults and are one of the most frequent non-rhabdomyosarcomatous soft tissue tumors in pediatric age. These tumors usually occur in young adults from a previously recognized neurofibroma, neurofibromatosis type 1 (NF1), with a noted change in size and pain. This child reached the age of 10 without the presence of the more commonly seen manifestations of NF1. Pseudoarthrosis in children has a high rate of association with NF1, and in this case diagnosis of NF1 was supported by development of MPNST in a pre-existing plexiform neurofibroma.
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